Selective behavioral and neurochemical effects of cholinergic lesions produced by intrabasalis infusions of 192 IgG-saporin on attentional performance in a five-choice serial reaction time task
192;
IgG-saporin;
attention;
in vivo microdialysis;
prefrontal cortex;
nucleus basalis magnocellularis;
basal forebrain;
D O I:
10.1523/JNEUROSCI.22-05-01905.2002
中图分类号:
Q189 [神经科学];
学科分类号:
071006 ;
摘要:
The effects of the cholinergic immunotoxin 192 IgG-saporin (SAP) (0.0, 0.15, or 0.45 mug/mul; 0.5 mul/hemisphere) infused into the area of the nucleus basalis magnocellularis (NBM) of rats were tested in a five-choice serial reaction time task (5CSRTT) designed to assess visual attention. The effects of this manipulation on acetylcholine efflux in the medial frontal cortex were determined using in vivo microdialysis during the 5CSRTT. Rats with extensive lesions of the NBM (SAP HIGH) showed an array of behavioral deficits in the 5CSRTT hypothesized to represent deficits in central executive function that were associated with severe deficits in accuracy. Lengthening the stimulus duration ameliorated these deficits. Rats with restricted lesions of the NBM (SAP LOW) showed impairments over time on task when tested under standard conditions that were exacerbated by increases in the event rate. The number of choline acetyl-transferase-immunoreactive cells in the area of the NBM but not the vertical limb of the diagonal band correlated significantly with accuracy in the task. SAP HIGH rats had significantly lower levels of cortical acetylcholine (ACh) efflux relative to SHAM both before and during the 5CSRTT. SAP LOW rats showed significantly higher levels of cortical ACh efflux before but not during the 5CSRTT. Cortical ACh efflux increased in all rats with the onset of the attentional task. These data provide the first direct evidence for a relationship between selective damage in the basal forebrain with decreased cortical ACh efflux and impaired attentional function.
机构:
Hokkaido Univ, Grad Sch Med, Dept Neuropharmacol, Kita Ku, Sapporo, Hokkaido 0608638, JapanHokkaido Univ, Grad Sch Med, Dept Neuropharmacol, Kita Ku, Sapporo, Hokkaido 0608638, Japan
Ohmura, Yu
Yamaguchi, Taku
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Hokkaido Univ, Grad Sch Med, Dept Neuropharmacol, Kita Ku, Sapporo, Hokkaido 0608638, JapanHokkaido Univ, Grad Sch Med, Dept Neuropharmacol, Kita Ku, Sapporo, Hokkaido 0608638, Japan
Yamaguchi, Taku
Futami, Yukino
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Hokkaido Univ, Grad Sch Med, Dept Neuropharmacol, Kita Ku, Sapporo, Hokkaido 0608638, JapanHokkaido Univ, Grad Sch Med, Dept Neuropharmacol, Kita Ku, Sapporo, Hokkaido 0608638, Japan
Futami, Yukino
Togashi, Hiroko
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Hokkaido Univ, Grad Sch Med, Dept Neuropharmacol, Kita Ku, Sapporo, Hokkaido 0608638, Japan
Hlth Sci Univ Hokkaido, Sch Pharmaceut Sci, Dept Pharmacol Sci, Ishikari, Hokkaido 0600293, JapanHokkaido Univ, Grad Sch Med, Dept Neuropharmacol, Kita Ku, Sapporo, Hokkaido 0608638, Japan
Togashi, Hiroko
Izumi, Takeshi
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Hokkaido Univ, Grad Sch Med, Dept Neuropharmacol, Kita Ku, Sapporo, Hokkaido 0608638, JapanHokkaido Univ, Grad Sch Med, Dept Neuropharmacol, Kita Ku, Sapporo, Hokkaido 0608638, Japan
Izumi, Takeshi
Matsumoto, Machiko
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Hokkaido Univ, Grad Sch Med, Dept Neuropharmacol, Kita Ku, Sapporo, Hokkaido 0608638, Japan
Hlth Sci Univ Hokkaido, Sch Pharmaceut Sci, Dept Pharmacol Sci, Ishikari, Hokkaido 0600293, JapanHokkaido Univ, Grad Sch Med, Dept Neuropharmacol, Kita Ku, Sapporo, Hokkaido 0608638, Japan
Matsumoto, Machiko
Yoshida, Takayuki
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Hokkaido Univ, Grad Sch Med, Dept Neuropharmacol, Kita Ku, Sapporo, Hokkaido 0608638, JapanHokkaido Univ, Grad Sch Med, Dept Neuropharmacol, Kita Ku, Sapporo, Hokkaido 0608638, Japan
Yoshida, Takayuki
Yoshioka, Mitsuhiro
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Hokkaido Univ, Grad Sch Med, Dept Neuropharmacol, Kita Ku, Sapporo, Hokkaido 0608638, JapanHokkaido Univ, Grad Sch Med, Dept Neuropharmacol, Kita Ku, Sapporo, Hokkaido 0608638, Japan